CLASS II Drug recall · Reported 28 Feb 2024 · FDA Enforcement Report

Meijer Cherry Cough Drops, Menthol cough suppressant/Oral recalled

Bestco is recalling Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per, distributed nationwide in the US. The recall was initiated on 19 Jan 2024 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes100042236, Exp 12/31/2026
Quantity recalled16 cases/4 pack each

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

Recall details

Recall number
D-0329-2024
FDA event ID
93869
Recalling firm
Bestco, Mooresville, NC
Classification
Class II
Status
Terminated
Recall initiated
19 Jan 2024
FDA classified
16 Feb 2024
Reported
28 Feb 2024
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Particulate Matter

Timeline

19 Jan 2024Recall initiated by company
16 Feb 2024Classified by FDA+28 days
28 Feb 2024Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

CGMP Deviations: Potential Glass and Silicone particulates in product

Product as listed by the FDA

Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per bag, item number 20000345, Bestco, 288 Mazeppa Road, Mooresville, NC 28115

Where it was distributed

Nationwide in the US

Nationwide

Stores named: Meijer

Questions about this recall

Is Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per recalled?

Yes. Bestco recalled Meijer Cherry Cough Drops, Menthol cough suppressant/Oral Anesthetic, 200 drops per on 19 Jan 2024. The recall is Class II and its status is Terminated. Recall number D-0329-2024.

Why was it recalled?

CGMP Deviations: Potential Glass and Silicone particulates in product

Which lots are affected?

100042236, Exp 12/31/2026

Where was it sold?

Nationwide in the US

What should I do if I have it?

Check the lot number on your package against the affected lots. If it matches, contact the pharmacy that dispensed it or your prescriber before stopping any medication.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

More recalls from Bestco

All 8